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782879004: Occipital pachygyria and polymicrogyria (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3756524017 Occipital pachygyria and polymicrogyria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3756525016 Occipital pachygyria and polymicrogyria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3756526015 Occipital MCD (malformation of cortical development) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3756527012 A rare genetic cerebral malformation characterized by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalized tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3756528019 A rare genetic cerebral malformation characterised by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalised tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4045011000172119 occipitale pachygyrie en polymicrogyrie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4045021000172112 occipitale macrogyrie en polymicrogyrie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Occipital pachygyria and polymicrogyria (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Occipital pachygyria and polymicrogyria (disorder) Is a Microgyria true Inferred relationship Some
Occipital pachygyria and polymicrogyria (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Occipital pachygyria and polymicrogyria (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Occipital pachygyria and polymicrogyria (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Occipital pachygyria and polymicrogyria (disorder) Occurrence Congenital true Inferred relationship Some 1
Occipital pachygyria and polymicrogyria (disorder) Finding site Structure of occipital lobe gyrus (body structure) true Inferred relationship Some 2
Occipital pachygyria and polymicrogyria (disorder) Occurrence Congenital true Inferred relationship Some 2
Occipital pachygyria and polymicrogyria (disorder) Finding site Structure of occipital lobe gyrus (body structure) true Inferred relationship Some 1
Occipital pachygyria and polymicrogyria (disorder) Is a Macrogyria true Inferred relationship Some
Occipital pachygyria and polymicrogyria (disorder) Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 2
Occipital pachygyria and polymicrogyria (disorder) Associated morphology Congenital smallness true Inferred relationship Some 1
Occipital pachygyria and polymicrogyria (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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